Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
FRONTONASAL DYSPLASIA - SEVERE MICROPHTHALMIA - SEVERE FACIAL CLEFTING SYNDROME
MONDO:0013271
ALX1 Causal
20451171 27324866 23059813 32914578 26610632
ClinGen, ClinVar, GWAS catalog —
All1 Causal1 Unknown1
Related Diseases Diseases that share the most curated genes with Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome.
3 View disease cluster →
Frontonasal dysplasia 1 shared geneALX1 Related via 1 shared gene including ALX1. Craniofacial abnormalities 1 shared geneALX1 Related via 1 shared gene including ALX1. Desbuquois syndrome 1 shared geneALX1 Related via 1 shared gene including ALX1.